X-linked recessive aqueductal stenosis without macrocephaly

Clin Genet. 1988 May;33(5):390-4. doi: 10.1111/j.1399-0004.1988.tb03467.x.

Abstract

A normocephalic, severely retarded boy with a family history suggesting aqueductal stenosis was found by computerized tomography to have aqueductal stenosis. His parents' concurrent pregnancy was monitored by ultrasonography and amniocentesis; these disclosed a male fetus which developed marked hydrocephalus after the 20th week. The pregnancy was terminated and an autopsy of the fetus demonstrated several major CNS malformations in addition to a very narrowed aqueduct. This case illustrates the diffuse CNS disease present in at least some cases of X-linked aqueductal stenosis (XLAS) and the importance of considering this variable syndrome in normocephalic, non-dysmorphic mentally retarded males. Important aspects of the prenatal diagnosis of XLAS are also illustrated.

Publication types

  • Case Reports

MeSH terms

  • Cerebral Aqueduct / abnormalities*
  • Child
  • Female
  • Fetal Diseases / diagnosis
  • Fetal Diseases / genetics
  • Genes, Recessive
  • Humans
  • Hydrocephalus / diagnosis
  • Hydrocephalus / genetics*
  • Intellectual Disability / genetics*
  • Male
  • Pedigree
  • Pregnancy
  • Prenatal Diagnosis
  • X Chromosome